C0342739[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3220931	NM_001002294.3(FMO3):c.601A>C (p.Thr201Pro)	FMO3, LOC126805916 (T138P +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GLikely benign
Select item 3064195	NM_001002294.3(FMO3):c.828-2A>G	FMO3	Single nucleotide variant (splice acceptor variant)	Trimethylaminuria	GLikely pathogenic
Select item 38395	NM_001002294.3(FMO3):c.923A>G (p.Glu308Gly)	FMO3 (E308G +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 631576	NM_001002294.3(FMO3):c.929C>T (p.Ser310Leu)	FMO3 (S310L +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +2 more	GLikely pathogenic
Select item 3064094	NM_002022.3(FMO4):c.83C>A (p.Pro28His)	FMO4 (P28H)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance

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